Methanol → HCID 12799944, compound
Reaction equation
B.[C:2]([C:15]1[C:23]2[C:18](=[CH:19][C:20]([C:24]([O:26][CH3:27])=[O:25])=[CH:21][CH:22]=2)[NH:17][CH:16]=1)(=O)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13].C(OCC)(=O)C.CO>O1CCCC1.O>[CH2:2]([C:15]1[C:23]2[C:18](=[CH:19][C:20]([C:24]([O:26][CH3:27])=[O:25])=[CH:21][CH:22]=2)[NH:17][CH:16]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH3:13]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 50 °C
Procedure
A solution of borane in tetrahydrofuran (134 ml, of strength 1M) in portions (13×10 ml) was added during 20 minutes to a stirred solution of methyl 3-(n-dodecanoyl)indole-6-carboxylate (19.9 g) in a mixture of dry tetrahydrofuran (330 ml) and dry ethyl acetate (330 ml), the temperature of the reaction being maintained at 50° C. by external warming. The mixture was stirred and refluxed for 1.5 hours and then methanol (330 ml) was added to the refluxing mixture during 10 minutes. The mixture was refluxed for a further 30 minutes and water (50 ml) was added. The mixture was distilled at atmospheric pressure to remove the organic solvents to give a yellow residue. The residue was triturated with water (50 ml) to give a solid, which was collected and washed with water (100 ml). The solid was recrystallised from methanol (100 ml) (with treatment with charcoal) and then from toluene to give methyl 3-(n-dodecyl)-indole-6-carboxylate (10 g), in the form of a white solid, m.p. 85°-89° C.
Workup
- temperaturerefluxed for 1.5 hours
- temperatureThe mixture was refluxed for a further 30 minutes
- distillationThe mixture was distilled at atmospheric pressure
- customto remove the organic solvents
- customto give a yellow residue
- customThe residue was triturated with water (50 ml)
- customto give a solid, which
- customwas collected
- washwashed with water (100 ml)
- customThe solid was recrystallised from methanol (100 ml) (with treatment with charcoal)
Sources & evidence
- ORD record
- ord-fd1e0697e0034b3c93dc7aa7cadb82db
- Source dataset
- uspto-grants-1985_01
- Patent number
- US04493843
Reaction notes
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